Senior QC analyst

Quanta part of QCS Staffing; Cork; On-site; EUR 50,000 - 70,000; Full time

Job summary

A global pharmaceutical client near Cork is seeking a Senior QC Analyst to join their team. The role involves leading cross-functional projects and applying knowledge of analytical techniques in a GMP environment. The ideal candidate will have a BSc/MSc in Science, extensive experience with chemistry techniques, and a focus on method validation. This is a contract position in a growth-focused site.

Qualifications

• Extensive experience working with chemistry techniques in a QC/Analytical role.
• Knowledge of protein chemistry and analytical techniques in a GMP environment.

Responsibilities

• Lead and participate in cross-functional projects.
• Apply knowledge of protein chemistry in a Chemistry Separations laboratory.
• Review and approve technical documents and procedures.

Skills

Analytical techniques

Protein chemistry

Method validation

Troubleshooting

Education

BSc/MSc in Science or related field

Tools

HPLC

CE

Job description

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Senior QC Analyst - Life Sciences – Contract - Ireland

One of our global pharmaceutical clients is looking for a Senior QC Analyst to join their team near the picturesque city of Cork. The site is renowned for manufacturing excellence and plays a vital role in the company's large-scale biotech operations worldwide.

The site has received significant investment over the last five years to support growth and expansion. With new products coming to the site, it is an exciting time to join the team.

Essential Duties and Responsibilities include, but are not limited to:

1. Lead and participate in cross-functional projects, troubleshooting teams, and investigations across the site.
2. Apply knowledge of protein chemistry and analytical techniques in a Chemistry Separations laboratory (e.g., HPLC, CE, protein biochemistry), including method validations, transfers, and equipment qualifications in a GMP environment.
3. Perform laboratory experiments to meet project timelines.
4. Contribute to continuous improvement initiatives, including method optimization and troubleshooting.
5. Prepare documentation related to projects in accordance with GDP and site procedures.
6. Review and approve technical documents, procedures, CAPAs, change controls, deviations, and metrics.

Requirements:

• BSc/MSc in Science or related field.
• Extensive experience working with chemistry techniques (e.g., HPLC, CE, protein biochemistry) in a QC/Analytical role.
• Knowledge of protein chemistry, analytical techniques, method validation, transfers, and equipment qualification in a GMP environment.

If you are interested, please apply now for more information!

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